Catalog |
name |
Description |
price |
R-M3-1019 |
2-Acetamido-5-aminophenylboronic acid,CAS:136237-84-8 |
2-Acetamido-5-aminophenylboronic acid/CAS:136237-84-8 is a versatile compound with valuable applications in medicinal chemistry, organic synthesis, and biochemical research.As a phenylboronic acid derivative, it is used in organic synthesis reactions, particularly in Suzuki coupling reactions to form carbon-carbon bonds. |
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R-M3-1020 |
CAS1212508-82-1 |
Given the complexity and presence of specific functional groups, this compound could have potential applications as an antagonist or agonist at specific receptors in the nervous system. |
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R-M3-1021 |
2-(Acetyloxy)-1,2,3-propanetricarboxylic Acid 1,2-Dibutyl Ester,CAS:2097561-44-7 |
2-(Acetyloxy)-1,2,3-propanetricarboxylic Acid 1,2-Dibutyl Ester is an esterified derivative of citric acid, modified with acetoxy and butyl groups, which might lend it various biochemical properties and potential industrial applications.Compounds derived from citric acid are commonly used in biochemistry as they can function as metabolic intermediates.Esters of citric acid and its derivatives are often used as food additives and flavoring agents.These types of esters might also have applications in drug delivery systems. |
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R-M3-1022 |
5-Acetyl-d3-amino-6-formylamino-3-methyluracil,CAS:1185082-65-8 |
5-Acetyl-d3-amino-6-formylamino-3-methyluracil,CAS:1185082-65-8 are often utilized in studies of nucleobase modifications, RNA structure, and function.Modified nucleobases can serve as potential drugs or biomarkers due to their altered molecular properties, which might lead to new therapeutic agents. |
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R-M3-1023 |
5-[(6-O-Acetyl-β-D-galactopyranosyl)oxy]-7-hydroxy-4-(4-hydroxyphenyl)-2H-1-benzopyran-2-one |
5-[(6-O-Acetyl-β-D-galactopyranosyl)oxy]-7-hydroxy-4-(4-hydroxyphenyl)-2H-1-benzopyran-2-one represents a chemically modified flavonoid structure. Such compounds may be significant in medicinal chemistry, pharmacology, and natural product chemistry. |
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R-M3-1024 |
5-[(6-O-Acetyl-β-D-galactopyranosyl)oxy]-4-(3,4-dihydroxyphenyl)-7-hydroxy-2H-1-benzopyran-2-one |
5-[(6-O-Acetyl-β-D-galactopyranosyl)oxy]-4-(3,4-dihydroxyphenyl)-7-hydroxy-2H-1-benzopyran-2-one may have biological activities and could be investigated for applications in pharmacology or biochemistry, particularly due to the presence of phenolic and glycosidic structures that are often associated with antioxidant and health-benefitting properties. |
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R-M3-125 |
Cas203252-14-6 |
(3R,4R)-4-(Acetyloxy)-3-[(1R)-1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethyl]-1-(4-methoxyphenyl)-2-azetidinone containing azetidinone cores often exhibit biological activity and could be of interest in medicinal chemistry. The functional groups present — the acetoxy, methoxy phenyl group, and silyl ether — may impart specific physical and chemical properties, potentially influencing the compound’s solubility, reactivity, and biological interactions. |
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R-M3-126 |
(2S,4R)-4-(Acetylthio)-2-[[(aminosulfonyl)[(1,1-dimethylethoxy)carbonyl]amino]methyl]-1-pyrrolidinec |
(2S,4R)-4-(Acetylthio)-2-[[(aminosulfonyl)[(1,1-dimethylethoxy)carbonyl]amino]methyl]-1-pyrrolidinecarboxylic Acid (4-Nitrophenyl) Ethyl Ester is a complex organic molecule with several significant functional groups and stereochemistry. Compounds like this could be of interest in medicinal chemistry due to the presence of multiple biological motifs such as the pyrrolidine structure, the aminosulfonyl group, and the carboxylic acid. The presence of the nitro group and the thioester group may also indicate potential pharmacological activities. |
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R-M3-128 |
Acrinathrin,CAS:101007-06-1 |
Acrinathrin is a potent insecticide with a well-defined mechanism of action targeting the nervous systems of insects, making it effective for agricultural pest control. |
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R-M3-129 |
Acrivastine Isomer Z,CAS:1057138-89-2 |
Acrivastine is an antihistamine commonly used for the relief of allergy symptoms such as hay fever, urticaria (hives), and rhinitis. It is a second-generation antihistamine that is effective in blocking the action of histamine at the H1 receptor sites. |
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